Congenital cataract

Symptom Information:

Symptom ID: HPO:0000519
Synonyms:
Bilateral cataracts [HPO:0000519]
Bilateral congenital cataracts [HPO:0000519]
Cataract, congenital [HPO:0000519]
Cataracts, lenticular, bilateral [HPO:0000519]
Congenital cataracts [HPO:0000519]
Congenital cataracts, bilateral [HPO:0000519]
Bilateral cataracts [OMIM:Bilateral cataracts]
Bilateral congenital cataracts [OMIM:Bilateral congenital cataracts]
Cataract, congenital [OMIM:Cataract, congenital]
Cataracts, lenticular, bilateral [OMIM:Cataracts, lenticular, bilateral]
Congenital cataract [OMIM:Congenital cataract]
Congenital cataracts [OMIM:Congenital cataracts]
Bilateral congenital cataracts (males) [OMIM:Bilateral congenital cataracts (males)]
Cataract, congenital (in some patients) [OMIM:Cataract, congenital (in some patients)]
Cataract, congenital (nuclear, sutural, or stellate cortical) [OMIM:Cataract, congenital (nuclear, sutural, or stellate cortical)]
Cataract, congenital (rare) [OMIM:Cataract, congenital (rare)]
Cataracts, congenital [OMIM:Cataracts, congenital]
Cataracts, congenital (in some patients) [OMIM:Cataracts, congenital (in some patients)]
Congenital cataract (males) [OMIM:Congenital cataract (males)]
Congenital cataracts (1 family) [OMIM:Congenital cataracts (1 family)]
Congenital cataracts (rare) [OMIM:Congenital cataracts (rare)]
Congenital cataracts (reported in 1 family) [OMIM:Congenital cataracts (reported in 1 family)]
Congenital cataracts (reported in 1 patient) [OMIM:Congenital cataracts (reported in 1 patient)]
Cataract congenital [MedDRA:10007747]
Quality:
Cross references:
OMIM: "Bilateral cataracts" [OMIM:Bilateral cataracts]
OMIM: "Bilateral congenital cataracts" [OMIM:Bilateral congenital cataracts]
OMIM: "Cataract, congenital" [OMIM:Cataract, congenital]
OMIM: "Cataracts, lenticular, bilateral" [OMIM:Cataracts, lenticular, bilateral]
OMIM: "Congenital cataract" [OMIM:Congenital cataract]
OMIM: "Congenital cataracts" [OMIM:Congenital cataracts]
OMIM: "Bilateral congenital cataracts (males)" [OMIM:Bilateral congenital cataracts (males)]
OMIM: "Cataract, congenital (in some patients)" [OMIM:Cataract, congenital (in some patients)]
OMIM: "Cataract, congenital (nuclear, sutural, or stellate cortical)" [OMIM:Cataract, congenital (nuclear, sutural, or stellate cortical)]
OMIM: "Cataract, congenital (rare)" [OMIM:Cataract, congenital (rare)]
OMIM: "Cataracts, congenital" [OMIM:Cataracts, congenital]
OMIM: "Cataracts, congenital (in some patients)" [OMIM:Cataracts, congenital (in some patients)]
OMIM: "Congenital cataract (males)" [OMIM:Congenital cataract (males)]
OMIM: "Congenital cataracts (1 family)" [OMIM:Congenital cataracts (1 family)]
OMIM: "Congenital cataracts (rare)" [OMIM:Congenital cataracts (rare)]
OMIM: "Congenital cataracts (reported in 1 family)" [OMIM:Congenital cataracts (reported in 1 family)]
OMIM: "Congenital cataracts (reported in 1 patient)" [OMIM:Congenital cataracts (reported in 1 patient)]
Is a (Direct Parents):
MedDRA Rubella viral infections
HPO         Cataract
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the eye(HPO:0000478)
          Abnormal eye morphology(HPO:0012372)
             Abnormality of the globe(HPO:0012374)
                Abnormality of the anterior segment of the globe(HPO:0004328)
                   Abnormality of the lens(HPO:0000517)
                      Cataract(HPO:0000518)
                         Congenital cataract(HPO:0000519)
MedDRA:
Infections and infestations(MedDRA:10021881)
    Viral infectious disorders(MedDRA:10047438)
       Rubella viral infections(MedDRA:10039270)
          Congenital cataract(HPO:0000519)
Database Frequency: 73 / 7739
Resource:

All diseases associated with this symptom:

3-phosphoglycerate dehydrogenase deficiency (Orphanet:79351)
ADAMS-OLIVER SYNDROME 2 (OMIM:614219)
ATAXIA-MICROCEPHALY-CATARACT SYNDROME (OMIM:208870)
Absence deformity of leg - cataract (Orphanet:2310)
Autosomal dominant Kenny-Caffey syndrome (Orphanet:93325)
Autosomal recessive palmoplantar keratoderma and congenital alopecia (Orphanet:1366)
Autosomal recessive spastic paraplegia type 45 (Orphanet:320396)
Autosomal recessive spastic paraplegia type 46 (Orphanet:320391)
CARDIOFACIOCUTANEOUS SYNDROME 4 (OMIM:615280)
CATARACT 1, MULTIPLE TYPES (OMIM:116200)
CATARACT 10, MULTIPLE TYPES (OMIM:600881)
CATARACT 16, MULTIPLE TYPES (OMIM:613763)
CATARACT 17, MULTIPLE TYPES (OMIM:611544)
CATARACT 3, MULTIPLE TYPES (OMIM:601547)
CATARACT 37 (OMIM:614422)
CATARACT 38 (OMIM:614691)
CATARACT 39, MULTIPLE TYPES (OMIM:615188)
CATARACT 4, MULTIPLE TYPES (OMIM:115700)
CATARACT 41 (OMIM:116400)
CATARACT 42 (OMIM:115900)
CATARACT 6, MULTIPLE TYPES (OMIM:116600)
CATARACT, CONGENITAL, WITH MENTAL IMPAIRMENT AND DENTATE GYRUS ATROPHY (OMIM:607674)
CATARACT, TOTAL CONGENITAL (OMIM:116700)
CATARACTS, CONGENITAL, WITH SENSORINEURAL DEAFNESS, DOWN SYNDROME-LIKEFACIAL APPEARANCE, SHORT STATURE, AND MENTAL RETARDATION (OMIM:601088)
CODAS syndrome (Orphanet:1458)
Cataract - ataxia - deafness (Orphanet:1368)
Cataract - nephropathy - encephalopathy (Orphanet:1380)
Cataract with Y-shaped suture opacities (Orphanet:98985)
Cataract, Coppock-like (Orphanet:98986)
Cataract, Hutterite type (Orphanet:98987)
Cataract-microcornea syndrome (Orphanet:1377)
Congenital cataract, Volkmann type (Orphanet:98983)
Congenital cataract-hearing loss-severe developmental delay syndrome (Orphanet:300313)
Congenital cataract-hypertrophic cardiomyopathy-mitochondrial myopathy syndrome (Orphanet:1369)
Congenital cataracts - facial dysmorphism - neuropathy (Orphanet:48431)
Congenital osteogenesis imperfecta - microcephaly - cataracts (Orphanet:2772)
Early-onset non-syndromic cataract (Orphanet:217052)
FECHTNER SYNDROME (OMIM:153640)
Familial vascular leukoencephalopathy (Orphanet:36383)
GROWTH FAILURE, MICROCEPHALY, MENTAL RETARDATION, CATARACTS, LARGEJOINT CONTRACTURES, OSTEOPOROSIS, CORTICAL DYSPLASIA, AND CEREBELLARATROPHY (OMIM:608278)
HEC syndrome (Orphanet:2119)
Hypomyelination - congenital cataract (Orphanet:85163)
Kenny-Caffey syndrome (Orphanet:2333)
Knobloch syndrome (Orphanet:1571)
MELAS (Orphanet:550)
MOVED TO 302200 (OMIM:302300)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION),TYPE B, 1 (OMIM:613155)
Marinesco-Sjögren syndrome (Orphanet:559)
Marshall syndrome (Orphanet:560)
Micro syndrome (Orphanet:2510)
Multiple acyl-CoA dehydrogenase deficiency (Orphanet:26791)
Nance-Horan syndrome (Orphanet:627)
Oculocerebrorenal syndrome (Orphanet:534)
Oculofaciocardiodental syndrome (Orphanet:2712)
PARTIAL LIPODYSTROPHY, CONGENITAL CATARACTS, AND NEURODEGENERATIONSYNDROME (OMIM:606721)
PEROXISOME BIOGENESIS DISORDER 14B (OMIM:614920)
PHACE syndrome (Orphanet:42775)
PHEOCHROMOCYTOMAPHEOCHROMOCYTOMA, SUSCEPTIBILITY TO (OMIM:171300)
PUPILLARY MEMBRANE, PERSISTENCE OF (OMIM:178900)
Partial congenital cataract (Orphanet:98992)
Porencephaly-microcephaly-bilateral congenital cataract syndrome (Orphanet:306547)
RETINITIS PIGMENTOSA 62 (OMIM:614181)
Rhizomelic chondrodysplasia punctata (Orphanet:177)
Rhizomelic chondrodysplasia punctata type 1 (Orphanet:309789)
Scalp-ear-nipple syndrome (Orphanet:2036)
Spastic ataxia - corneal dystrophy (Orphanet:2572)
Spastic paraplegia 64, autosomal recessive (OMIM:615683)
Vici syndrome (Orphanet:1493)
WARBURG MICRO SYNDROME 1 (OMIM:600118)
WARBURG MICRO SYNDROME 2 (OMIM:614225)
WARBURG MICRO SYNDROME 4 (OMIM:615663)
X-linked Alport syndrome (Orphanet:88917)
[DEL] SENGERS SYNDROME (OMIM:212350)